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rs863225396

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863225396(G;T)
Make rs863225396(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position47480731
GeneMSH2
is asnp
is mentioned by
dbSNPrs863225396
ebirs863225396
HLIrs863225396
Exacrs863225396
Varsomers863225396
Maprs863225396
PheGenIrs863225396
hapmaprs863225396
1000 genomesrs863225396
hgdprs863225396
ensemblrs863225396
gopubmedrs863225396
geneviewrs863225396
scholarrs863225396
googlers863225396
pharmgkbrs863225396
gwascentralrs863225396
openSNPrs863225396
23andMers863225396
23andMe allrs863225396
SNP Nexus

SNPshotrs863225396
SNPdbers863225396
MSV3drs863225396
GWAS Ctlgrs863225396
Max Magnitude0
ClinVar
Risk rs863225396(T;T)
Alt rs863225396(T;T)
Reference rs863225396(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MSH2
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.47707870G>T
CLNSRC
CLNACC RCV000201967.1,